ERCC6 Chromosome 10

ERCC excision repair 6, chromatin remodeling factor
413 variants 413 Health Risk

Upload your DNA to see your personal genotypes for variants in ERCC6.

What This Gene Does
This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]
Gene Info
Gene Group
"SNF2 related family|ERCC excision repair associated|B-WICH chromatin-remodelling complex subunits"
Locus Type
gene with protein product
Location
10q11.23
Ensembl
ENSG00000225830
Associated Conditions (28)
Cockayne syndrome
Cerebrooculofacioskeletal syndrome 1
ERCC6-related disorder
Age related macular degeneration 5
Cockayne syndrome type 2
Inborn genetic diseases
Thymoma
DE SANCTIS-CACCHIONE SYNDROME
Hereditary breast ovarian cancer syndrome
7 conditions
Cone-rod dystrophy
Intellectual disability
6 conditions
Clear cell carcinoma of kidney
Uveal melanoma
Colon adenocarcinoma
Melanoma
Malignant tumor of esophagus
Familial cancer of breast
Ovarian serous cystadenocarcinoma
+8 more conditions
Key Variants
RS1057518910
Conflicting classifications of pathogenicity
Cockayne syndrome, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome
Health Risk
RS114234514
Conflicting classifications of pathogenicity
ERCC6-related disorder, ERCC6-related disorder
Health Risk
RS114403790
Conflicting classifications of pathogenicity
Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
Health Risk
RS114490473
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS114832108
Conflicting classifications of pathogenicity
Health Risk
RS115633798
Conflicting classifications of pathogenicity
Inborn genetic diseases, Thymoma, Inborn genetic diseases
Health Risk
RS115643329
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS115875661
Conflicting classifications of pathogenicity
Health Risk
RS115876786
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS116032070
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS1163269726
Conflicting classifications of pathogenicity
Inborn genetic diseases, Cockayne syndrome type 2, Inborn genetic diseases
Health Risk
RS117555054
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
All Variants (413)
RSID Category Clinical Significance Conditions
RS1057518910 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome
RS114234514 Health Risk Conflicting classifications of pathogenicity ERCC6-related disorder, ERCC6-related disorder
RS114403790 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS114490473 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS114832108 Health Risk Conflicting classifications of pathogenicity
RS115633798 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Thymoma, Inborn genetic diseases
RS115643329 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS115875661 Health Risk Conflicting classifications of pathogenicity
RS115876786 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS116032070 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS1163269726 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Cockayne syndrome type 2, Inborn genetic diseases
RS117555054 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS1275257135 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cockayne syndrome type 2
RS1317145066 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, DE SANCTIS-CACCHIONE SYNDROME, Cockayne syndrome type 2
RS1349103905 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cockayne syndrome type 2
RS138756386 Health Risk Conflicting classifications of pathogenicity
RS138758064 Health Risk Conflicting classifications of pathogenicity Hereditary breast ovarian cancer syndrome, Hereditary breast ovarian cancer syndrome
RS138865542 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS139007661 Health Risk Conflicting classifications of pathogenicity 7 conditions, DE SANCTIS-CACCHIONE SYNDROME, Inborn genetic diseases
RS139188695 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS141121035 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS141391984 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS142097249 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1421008948 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142219494 Health Risk Conflicting classifications of pathogenicity ERCC6-related disorder, ERCC6-related disorder
RS142580756 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS142641602 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS143260457 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS144608959 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1
RS145554525 Health Risk Conflicting classifications of pathogenicity
RS145720191 Health Risk Conflicting classifications of pathogenicity ERCC6-related disorder, Clear cell carcinoma of kidney, Uveal melanoma
RS146043988 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1
RS146165518 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1
RS146690522 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS147079519 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS147637331 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS148095899 Health Risk Conflicting classifications of pathogenicity
RS148295935 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS148475034 Health Risk Conflicting classifications of pathogenicity
RS148845653 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS149382642 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1
RS150065567 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150277901 Health Risk Conflicting classifications of pathogenicity
RS150762517 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS150935953 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS1590405627 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome, Cockayne syndrome
RS181327678 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS1837452924 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS1850797114 Health Risk Conflicting classifications of pathogenicity 7 conditions, Magnetic resonance imaging of brain abnormal, Intellectual disability
RS186482480 Health Risk Conflicting classifications of pathogenicity DE SANCTIS-CACCHIONE SYNDROME, ERCC6-related disorder, DE SANCTIS-CACCHIONE SYNDROME
1 2 3 4 ... 9 Next »
Sign Up to Analyze Your DNA Log In